A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052282



Internal ID18794813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30094196..30608663hg38UCSC Ensembl
Innerchr15:30386399..30900866hg19UCSC Ensembl
Innerchr15:28173691..28688158hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38514468
hg19514468
hg18514468
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2500n100
Supporting Variantsnssv3546453, nssv3546458, nssv3546457, nssv3546455, nssv3721487, nssv3546454, nssv3546456, nssv3721485, nssv3721486, nssv3721484
Samples
Known GenesCHRFAM7A, DKFZP434L187, GOLGA8H, GOLGA8J, GOLGA8T, LOC101059918, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052282
Frequency
Sample Size29084
Observed Gain1
Observed Loss9
Observed Complex0
Frequencyn/a


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